DRAD3000E/RADREX-I— 510(k) K082494
Substantially EquivalentToshiba America Medical Systems, In.C
FDA 510(k) clearance K082494 for DRAD3000E/RADREX-I, Substantially Equivalent on 2008-09-12. Applicant: Toshiba America Medical Systems, In.C.
Clearance details
- Applicant
- Toshiba America Medical Systems, In.C
- Product code
- Code MQB
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Tustin, CA, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.